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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5543985insertion1nstd206human GRCh38 chr3: 51,987,142-51,987,178 , GRCh37.p13 chr3: 52,021,158-52,021,194 ABHD14A-ACY1, ACY1
    nsv5453783copy number variation1nstd206human GRCh38 chr3: 51,988,218-51,993,093 , GRCh37.p13 chr3: 52,022,234-52,027,109 ACY1, RPL29, 1 more genes
    nsv5450606copy number variation1nstd206human GRCh38 chr3: 51,981,914-51,982,392 , GRCh37.p13 chr3: 52,015,930-52,016,408 ABHD14A-ACY1, ACY1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4914341copy number variation1nstd200human GRCh38 chr3: 51,964,147-51,987,926 , GRCh37.p13 chr3: 51,998,163-52,021,942 ABHD14B, ABHD14A-ACY1, 3 more genes
    nsv4911359copy number variation1nstd200human GRCh38 chr3: 51,972,365-51,981,974 , GRCh37.p13 chr3: 52,006,381-52,015,990 ABHD14A-ACY1, ACY1, 2 more genes
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
    nsv4728314copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,975,459-52,561,678 , GRCh38.p12 chr3: 51,941,443-52,527,662 ABHD14A-ACY1, POC1A, 32 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4386176copy number variation1nstd173human GRCh37 chr3: 52,005,891-52,028,350 , GRCh38.p12 chr3: 51,971,875-51,994,334 RPL29, ABHD14A-ACY1, 3 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4077200copy number variation1nstd166human GRCh37.p13 chr3: 52,018,276-52,021,816 , GRCh38.p12 chr3: 51,984,260-51,987,800 ACY1, ABHD14A-ACY1
    nsv4076800copy number variation1nstd166human GRCh37.p13 chr3: 52,006,383-52,015,996 , GRCh38.p12 chr3: 51,972,367-51,981,980 ABHD14B, ABHD14A, 2 more genes
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